A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586844



Internal ID20959915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:58681636..58682395hg38UCSC Ensembl
chr10:60441396..60442155hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38760
hg19760
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218642
Samples
Known GenesBICC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586844
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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